MAPKAPK3 MAPK activated protein kinase 3
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 2 |
| Benign | 0 | 14 |
| Likely benign | 0 | 172 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| risk factor | 0 | 2 |
| Uncertain significance | 0 | 300 |
Ranking
| ClinVar | |
|---|---|
![]() |
0 |
![]() |
0 |
![]() |
18 |
![]() |
468 |
![]() |
4 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | 3PK |
| SYNONYM | MAPKAP-K3 |
| SYNONYM | MAPKAP3 |
| SYNONYM | MAPKAPK-3 |
| SYNONYM | MDPT3 |
| SYNONYM | MK-3 |
| SYNONYM | MK3 |
| MIM | 602130 OMIM |
| HGNC | HGNC:6888 HGNC |
| Ensembl | ENSG00000114738 Ensembl |
| AllianceGenome | HGNC:6888 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000446044.5 | hg38 | chr3 | 50,611,908 | 50,649,289 | 37,382 |
| ENST00000357955.6 | hg38 | chr3 | 50,617,170 | 50,649,288 | 32,119 |
| ENST00000621469.5 | hg38 | chr3 | 50,617,151 | 50,649,291 | 32,141 |
| ENST00000446044.5 | hg19 | chr3 | 50,649,339 | 50,686,720 | 37,382 |
| ENST00000621469.5 | hg19 | chr3 | 50,654,582 | 50,686,722 | 32,141 |
| ENST00000357955.6 | hg19 | chr3 | 50,654,601 | 50,686,719 | 32,119 |
Genome browser




